510(k) K003406 ยท FMI Needle, Hypodermic, Single Lumen
GUARDED NEEDLE 2000
| Applicant | International Medical Device Partners, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jan 12, 2001 |
| Received | Nov 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003406
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.